Universal tumor screening for lynch syndrome: perspectives of patients regarding willingness and informed consent

被引:6
作者
Subramonian, Anusree [1 ]
Smith, Doug
Dicks, Elizabeth [1 ]
Dawson, Lesa [2 ,3 ]
Borgaonkar, Mark [4 ]
Etchegary, Holly [1 ]
机构
[1] Mem Univ, Fac Med, Clin Epidemiol, St John, NF, Canada
[2] Mem Univ, Fac Med, Gynecol Oncol Womens Hlth & Genet, St John, NF, Canada
[3] Eastern Hlth, Womens Hlth & Genet, St John, NF, Canada
[4] Mem Univ, Fac Med, Gastroenterol, St John, NF, Canada
关键词
colorectal cancer; lynch syndrome; patient oriented research; reflex testing; universal tumor screening; REVISED BETHESDA GUIDELINES; GENETIC TESTING STRATEGIES; COLORECTAL-CANCER SYNDROME; MICROSATELLITE INSTABILITY; FAMILY COMMUNICATION; REDUCING MORBIDITY; COST-EFFECTIVENESS; CLINICAL-CRITERIA; RESPONSE RATES; PRIMARY-CARE;
D O I
10.2217/pme-2020-0026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim:Lynch Syndrome is associated with a significant risk of colorectal carcinoma (CRC) and other cancers. Universal tumor screening is a strategy to identify high-risk individuals by testing all CRC tumors for molecular features suggestive of Lynch Syndrome. Patient interest in screening and preferences for consent have been underexplored.Methods:A postal survey was administered to CRC patients in a Canadian province.Results:Most patients (81.4%) were willing to have tumors tested if universal tumor screening were available and were willing to discuss test results with family members and healthcare professionals. The majority (62.6%) preferred informed consent be obtained prior to screening.Conclusion:Patients were supportive of universal screening. They expected consent to be obtained, contrary to current practice across Canada and elsewhere.
引用
收藏
页码:373 / 387
页数:15
相关论文
共 68 条
[31]   Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: Later age of onset [J].
Hampel, H ;
Stephens, JA ;
Pukkala, E ;
Sankila, R ;
Aaltonen, LA ;
Mecklin, JP ;
de la Chapelle, A .
GASTROENTEROLOGY, 2005, 129 (02) :415-421
[32]   Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives [J].
Hunter, Jessica Ezzell ;
Arnold, Kathleen A. ;
Cook, Jennifer E. ;
Zepp, Jamilyn ;
Gilmore, Marian J. ;
Rope, Alan F. ;
Davis, James V. ;
Bergen, Kellene M. ;
Esterberg, Elizabeth ;
Muessig, Kristin R. ;
Peterson, Susan K. ;
Syngal, Sapna ;
Acheson, Louise ;
Wiesner, Georgia ;
Reiss, Jacob ;
Goddard, Katrina A. B. .
FAMILIAL CANCER, 2017, 16 (03) :377-387
[33]   Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers [J].
Hunter, Jessica Ezzell ;
Zepp, Jamilyn M. ;
Gilmore, Mari J. ;
Davis, James V. ;
Esterberg, Elizabeth J. ;
Muessig, Kristin R. ;
Peterson, Susan K. ;
Syngal, Sapna ;
Acheson, Louise S. ;
Wiesner, Georgia L. ;
Reiss, Jacob A. ;
Goddard, Katrina A. B. .
CANCER, 2015, 121 (18) :3281-3289
[34]  
IBM Corporation IBM SPSS IBM Statistics IBMS IBM, 2016, IBM SPSS STAT 23 REL
[35]   Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening [J].
Julie, Catherine ;
Tresallet, Christophe ;
Brouquet, Antoine ;
Vallot, Celine ;
Zimmermann, Ute ;
Mitry, Emmanuel ;
Radvanyi, Francois ;
Rouleau, Etienne ;
Lidereau, Rosette ;
Coulet, Florence ;
Olschwang, Sylviane ;
Frebourg, Thierry ;
Rougier, Philippe ;
Nordlinger, Bernard ;
Laurent-Puig, Pierre ;
Penna, Christophe ;
Boileau, Catherine ;
Franc, Brigitte ;
Muti, Christine ;
Hofmann-Radvanyi, Helene .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (11) :2825-2835
[36]   Value of Genetic Testing for Hereditary Colorectal Cancer in a Probability-Based US Online Sample [J].
Knight, Sara J. ;
Mohamed, Ateesha F. ;
Marshall, Deborah A. ;
Ladabaum, Uri ;
Phillips, Kathryn A. ;
Walsh, Judith M. E. .
MEDICAL DECISION MAKING, 2015, 35 (06) :734-744
[37]   Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer A Cost-Effectiveness Analysis [J].
Ladabaum, Uri ;
Wang, Grace ;
Terdiman, Jonathan ;
Blanco, Amie ;
Kuppermann, Miriam ;
Boland, C. Richard ;
Ford, James ;
Elkin, Elena ;
Phillips, Kathryn A. .
ANNALS OF INTERNAL MEDICINE, 2011, 155 (02) :69-+
[38]   Genetic testing for Lynch syndrome: family communication and motivation [J].
Leenen, Celine H. M. ;
den Heijer, Mariska ;
van der Meer, Conny ;
Kuipers, Ernst J. ;
van Leerdam, Monique E. ;
Wagner, Anja .
FAMILIAL CANCER, 2016, 15 (01) :63-73
[39]   Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications [J].
Lynch, H. T. ;
Lynch, P. M. ;
Lanspa, S. J. ;
Snyder, C. L. ;
Lynch, J. F. ;
Boland, C. R. .
CLINICAL GENETICS, 2009, 76 (01) :1-18
[40]   Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications [J].
Lynch, HT ;
Boland, CR ;
Gong, G ;
Shaw, TG ;
Lynch, PM ;
Fodde, R ;
Lynch, JF ;
de la Chapelle, A .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (04) :390-402